BIOPAR DELTA-FORTE- 1 nf units, 50 mcg cbl, 2.5 mg f-thf, 1 mg pteglu-, 7 mg me-thf capsule

Drug Details [pdf]

DESCRIPTION

   [1 NF Units] [50 mcg CBl] [2.5 mg F-THf] [1 mg PteGlu-] [7 mg Me-THf]

   Prescription Hematopoietic Preparation For Therapeutic Use

   Multiphasic Softgels (30ct carton)

   NDC 64661-793-30
   Rx ONLY

   BioparTMdelta-FORTE is an orally administered prescription hematopoietic preparation for therapeutic use formulated for adult macrocytic anemia patients – specifically including pernicious anemia patients, ages 12 and up, who are under specific direction and monitoring of cobalamin and folate status by a physician.
INGREDIENTS

   Cobalamin-intrinsic factor concentrate (non-inhibitory)1 .............................................................................................. 1 NF Units§

   Adenosylcobalamin (coenzyme B12) .............................................................................................................................. 50 mcg

   Formyl folic acid, L-FTHf .............................................................................................................................................. 2.5 mg2

   Oxidized folic acid, DHf+ ................................................................................................................................................. 1 mg2

   Methyl folic acid, L-MeTHf ............................................................................................................................................... 7 mg2

      1 50 mcg Vitamin B12 (activity equivalent) and 50 mg of intrinsic factor concentrate§ from ultra-purified, porcine-derived stomach substance from a porcine, disease-free country; together these equal 1 NF Units. Cobalamin has hematopoietic activity apparently identical to that of the anti-anemia factor in purified liver-stomach extract

      2 Total folates is from l-methylfolate magnesium (molar equivalent) from amorphous, diastereoisomerically pure l-methylfolate (less than 1% d-isomer), DHF-dependent provitamin B9 (folic acid included) and the levo-isomer of folinic acid (label claim molar equivalent).
INACTIVES

ALSO CONTAINS:

      25 mg ascorbates4a (24 mg magnesium l-ascorbate, 1 mg zinc l-ascorbate) [antioxidant], 13.6 mg chelates (Cys-Fe3 as cysteinated pure amino acid chelate subsisting of 1.5 mg elemental iron4a) [colorant], phospholipids (phosphatidylserine-docosahexaenoic acid complex5)

OTHER INGREDIENTS:

      Annatto [colorant], betaine (trimethylglycine) [acidifier], citrates (citric acid, sodium citrate) [stabilizers], flavin adenine dinucleotide (B2-vitamer)4b, gelatin (bovine), glycerine, nicotinamide adenine dinucleotide hydride (B3-vitamer)4b, phospholipids (sunflower lecithin) [emulsifiers], piperine [bioavailability enhancer], purified water, pyridoxal 5’ phosphate (B6-vitamer)4b, thiamine pyrophosphate (B1-vitamer)4b, ubidecarenone [antioxidant], yellow beeswax.

      3 Pure amino acid, cysteinated iron chelate.

      4a 30% daily value (DV) of VITAMIN C, and 10% DV IRON for geriatric patients.

      4b Contains less than 2% (<25 mcg/each) of vitamins B1, B2, B3 and B6.

      5 Contains at least 12 mg phosphatidylserine (PS) – of which approximately 6.4 mg as PS-DHA, and less than 1% EPA (<800 mcg PS-EPA)
CONTAINS

FISH/KRILL/PORCINE (Intrinsic Factor/Cobalamin)/SOY

Certified 3rd-party GLUTEN-FREE. No artificial colorants. No dairy, wheat, sugar or egg
INDICATIONS & USAGE

BioparTM delta-FORTE is specifically indicated as a primary and adjunctive treatment in pernicious anemia patients having idiosyncrasy or sensitivity to parenteral administration - or when parental therapy is refused;
MECHANISM OF ACTION

COBALAMIN [TREATMENT]; FOLATE [PREVENTION]; INTRINSIC FACTOR [B12-ADJUVENT] -

Cobalamin is essential for the synthesis of methionine from homocysteine - a reaction which also requires folate. In the absence of cobalamin - ie, cobalamin deficiency, tetrahydrofolate cannot be regenerated from l-methylfolic acid, and a functional folate deficiency occurs - ie, “methyl trap hypothesis”. Gastrointestinal absorption of cobalamin depends on the presence of sufficient intrinsic factor, and lack of intrinisic factor results in cobalamin deficiency.
DOSAGE & ADMINISTRATION

   The adult dose is one capsule daily preferably on an empty stomach.

   A deficiency of cobalamin may present first as folate deficiency - which is why folate supplementation may mask the symptoms that would normally result and also why advanced folate supplementation requires licensed medical supervision; because of this, reticulocyte plasma count, cobalamin and folate must be obtained prior to treatment. Requirements of cobalamin and/or folate in excess of normal (due to pregnancy, thyrotoxicosis, hemolytic anemia, hemorrhage, malignancy, hepatic and renal disease) can usually be met with oral supplementation.

   As a general rule - in Pernicious Anemia patients, treatment will be required for the remainder of the patient’s life, and usually requires weekly or monthly injections at the doctor's office. Patients that are non-compliant with parenteral therapy (injections) may use this product as a substitute ONLY UNDER THE DIRECT SUPERVISION OF A LICENSED MEDICAL PRACTITIONER.
ADVERSE REACTIONS

Mild transient diarrhea, polycythemia vera, itching, transitory exanthema, feeling of swelling of entire body may occur with administration of cobalamin. Allergic sensitization has been reported following both oral and parenteral administration of folate.

Sensitivity to porcine intrinsic factor derived from liver substance has been reported in patients, and may occur at any time; BioparTMdelta-FORTE contains a non-inhibitory form of intrinsic factor that is not derived from liver substance but rather just the mucosa (stomach substance) - in which such senstitivity is less likely to occur, however caution is advised and continuous monitoring under licensed medical supervision is required.

BOXED WARNING (What is this?)

WARNING

USE OF THIS PRODUCT WITHOUT DIRECT SUPERVISION OF A PHYSICIAN IS DANGEROUS;
Some patients afflicted with pernicious anemia may or not respond to the orally ingested vitamin B12, and there is no known way to predict which patients may respond and which patients may cease to respond;
Periodic examinations and laboratory studies of pernicious anemia patients are essential and recommended; and -
The parenteral administration of (cyano)cobalamin - or vitamin B12, is generally recognized as a fully effective treatment of pernicious anemia. Parenteral alkyl-cobalamin preparations have not been and are not authorized for use except by or on the prescription of a physician.

PRECAUTIONS

GENERAL:

      0.1 mg or more of folic acid daily may obscure pernicious anemia in that the hematological remission may occur while neurological manifestations remain progressive. The safe tolerable limit for folic acid (in preparations) is 1 mg [emphasis added];

      Folic acid is not a substitute for vitamin B12 - although it may improve vitamin B12-deficient anemias. Exclusive use of folic acid in treating vitamin B12-deficient anemias could result in progressive and irreversible neurologic damage. Specifically, vitamin B12 deficiency allowed to progress over 3 months may produce permanent degenerative lesions of the spinal cord - as observed when folate therapy is used as the only hematopoietic agent;

      Doses of vitamin B12 exceeding 10 mcg daily may produce hematologic response in patients with folate deficiency. Indiscriminate administration may mask the true diagnosis; and -

      A dietary deficiency of only vitamin B12 is rare; multiple vitamin deficiency is expected in any dietary deficiency. No single regimen fits all cases, and the status of the patient observed in follow-up is the final criterion for adequacy of therapy.

DRUG INTERACTIONS:

      Colchicine, para-aminosalicylic acid, and heavy alcohol intake for longer than 2 weeks may produce malabsorption of cobalamin.

      Epileptic, antineoplastic and Parkinson's medications are cautioned in the concimant use with folate supplementation.
HOW SUPPLIED

BioparTM delta-FORTE is supplied as oval, annatto (”orangish-brown”) softgels* with imprint "7N3". Provided as a carton with 30 softgels in blister cards. NDC 64661-793-30.
REGULATORY

BioparTM delta-FORTE is regulated as a drug to ensure it's use is under medical supervision, and because of this, advanced folate supplementation is possible [21 CFR 250.201]. Intrinsic Factor was first marketed as Extralin(R) in 1932, and Extralin-B(R) with B-vitamins in 1936, followed by the Becotin(R) product which contained all the equivalent vitamins as this product plus intrinsic factor. "Old" drugs, including virtamins, which were considered safe prior to 1938, were permitted to continue on the market without further review. However, FDA maintained the authority to review these old drugs if possible safety concerns became apparent. In 1951, the Durham-Humphrey Act was passed. This act formally differentiated between prescription and OTC drugs. - 44 FR 16131 (March 16, 1979).
STORAGE AND HANDLING

   Call your medical practitioner about side effects. You may report side effects by calling (337) 662-5962.

   KEEP THIS OUT OF THE REACH OF CHILDREN.

   (Tamper Evident: Do not use if seal is broken or missing)

Do not exceed the recommended dose.

   STORAGE: Store at 20 ̊-25 ̊ C (68 ̊-77 ̊ F)

CAUTION: FEDERAL LAW PROHIBITS DISPENSING WITHOUT A PRESCRIPTION

[Rx ONLY]

PATENTS: Patent(s) pending.

TRADEMARKS: BioparTM delta-FORTEis a registered mark of JayMac Pharmaceuticals. DeltaFolateTM is a use-trademark of Jaymac Pharmaceuticals.

   JAYMAC Pharmaceuticals, LLC

   Sunset, LA 70584

   MANUFACTURED AND/OR PACKAGED IN USA/CANADA

   Revision

   Dec 28, 2021
CARTON IMAGES
PACKAGE INSERT
PILL/CAPSULE IMAGE
BLISTER CARD

INGREDIENTS AND APPEARANCE

BIOPAR DELTA-FORTE
1 nf units, 50 mcg cbl, 2.5 mg f-thf, 1 mg pteglu-, 7 mg me-thf capsule

Product Information
Product Type	HUMAN PRESCRIPTION DRUG	Item Code (Source)	NDC: 64661-793
Route of Administration	ORAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
INTRINSIC FACTOR (UNII: 70BT6OQT2Q) (INTRINSIC FACTOR - UNII:70BT6OQT2Q)	INTRINSIC FACTOR	50 mg
COBALAMIN (UNII: 8406EY2OQA) (COBALAMIN - UNII:8406EY2OQA)	COBALAMIN	50 ug
COBAMAMIDE (UNII: F0R1QK73KB) (COBAMAMIDE - UNII:F0R1QK73KB)	COBAMAMIDE	50 ug
levoLEUCOVORIN (UNII: 990S25980Y) (LEVOLEUCOVORIN - UNII:990S25980Y)	levoLEUCOVORIN	2.5 mg
DIHYDROFOLIC ACID (UNII: KXP0KNM559) (FOLIC ACID - UNII:935E97BOY8)	FOLIC ACID	1 mg
LEVOMEFOLATE MAGNESIUM (UNII: 1VZZ62R081) (LEVOMEFOLIC ACID - UNII:8S95DH25XC)	LEVOMEFOLIC ACID	7 mg

Ingredient Name	Strength
Inactive Ingredients
FERROUS CYSTEINE GLYCINATE (UNII: 8B4OP7RK5N)	13.6 mg
1,2-DOCOSAHEXANOYL-SN-GLYCERO-3-PHOSPHOSERINE CALCIUM (UNII: 6WJM73T46K)	6.4 mg
1,2-ICOSAPENTOYL-SN-GLYCERO-3-PHOSPHOSERINE CALCIUM (UNII: 9ABD9DRK7B)	800 ug
PHOSPHATIDYL SERINE (UNII: 394XK0IH40)	12 mg
PYRIDOXAL PHOSPHATE ANHYDROUS (UNII: F06SGE49M6)	25 ug
FLAVIN ADENINE DINUCLEOTIDE (UNII: ZC44YTI8KK)	25 ug
NADH (UNII: 4J24DQ0916)	25 ug
COCARBOXYLASE (UNII: Q57971654Y)	25 ug
MAGNESIUM ASCORBATE (UNII: 0N1G678593)	24 mg
ZINC ASCORBATE (UNII: 9TI35313XW)	1 mg
RIBOFLAVIN (UNII: TLM2976OFR)	5 mg
MAGNESIUM L-THREONATE (UNII: 1Y26ZZ0OTM)	1 mg
BETAINE (UNII: 3SCV180C9W)	500 ug
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)	1.83 mg
SODIUM CITRATE (UNII: 1Q73Q2JULR)	3.67 mg
ANNATTO (UNII: 6PQP1V1B6O)
GELATIN, UNSPECIFIED (UNII: 2G86QN327L)
GLYCERIN (UNII: PDC6A3C0OX)
LECITHIN, SUNFLOWER (UNII: 834K0WOS5G)
OLIVE OIL (UNII: 6UYK2W1W1E)
PIPERINE (UNII: U71XL721QK)
WATER (UNII: 059QF0KO0R)
UBIDECARENONE (UNII: EJ27X76M46)
YELLOW WAX (UNII: 2ZA36H0S2V)

Product Characteristics
Color	brown (ORANGISH-BROWN)	Score	no score
Shape	OVAL	Size	16mm
Flavor		Imprint Code	7N3
Contains

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC: 64661-793-30	30 in 1 CARTON	06/01/2024	06/01/2024
1		1 in 1 BLISTER PACK; Number of Units = 3; Type 0: Not a Combination Product

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
unapproved drug other		06/01/2024

Labeler - Jaymac Pharma (830767260)

Registrant - Jaymac Pharma (830767260)

Name	Address	ID/FEI	Business Operations
Establishment
Viva Pharmaceuticals INC		253288898	manufacture(64661-793)